Voorbeelden van het gebruik van Risk minimisation in het Engels en hun vertalingen in het Nederlands
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Computer
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Ecclesiastic
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Official/political
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Programming
Pharmacovigilance Plan or risk minimisation activities.
Criteria to be used to verify the success of proposed risk minimisation activity: Implementation of the education program will be monitored by the MAH via auditing.
has been adequately addressed through risk minimisation measures.
health care providers which is aimed at risk minimisation and to support safe
A training course for neurosurgeons which is aimed at risk minimisation and to support safe
Pharmacovigilance Plan or risk minimisation activities.
Pharmacovigilance Plan or risk minimisation activities.
The application is based on a reference medicinal product for which no safety concerns requiring additional risk minimisation activities have been identified.
Pharmacovigilance Plan or risk minimisation activities.
and adherence to the risk minimisation measures.
a system aimed to control distribution to IMLYGIC beyond the level of control ensured by routine risk minimisation measures.
and to optimize risk minimisation.
The MAH shall submit within 1 month of the Commission decision an updated Risk Management Plan which shall include a risk minimisation plan which includes additional risk minimisation measures to address the identified risks of bladder cancer and heart failure, as detailed below.
adequately addressed by risk minimisation measures for this medicine.
the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities• Within 60 days of an important(pharmacovigilance or risk minimisation) milestone being reached• At the request of the EMEA.
Pharmacovigilance Plan or risk minimisation activities• Within 60 days of an important(pharmacovigilance or risk minimisation) milestone being reached• At the request of the EMEA.
Pharmacovigilance Plan or risk minimisation activities• Within 60 days of an important(pharmacovigilance or risk minimisation) milestone being reached• At the request of the EMEA.
the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities• Within 60 days of an important(pharmacovigilance or risk minimisation) milestone being reached• At the request of the EMEA.